Quality Associate
Core
Hands-on Quality Associate supporting inspections, compliance, and continuous improvement in a regulated manufacturing environment.
Role type
Quality Associate (Manufacturing)
Builds
Quality operations and compliance within a regulated manufacturing business
Domain
Manufacturing (Medical Devices/Pharma)
Required skills
Inspection of materials and finished goods, Non-conforming material management, QMS compliance, Customer complaint handling, Audit documentation, MRB coordination, Supplier quality investigation, CAPA processes, SOP training
Preferred skills
Engineering drawings interpretation, Inspection tool usage, Cross-functional communication
Technologies
Microsoft Office, ERP systems, ISO 13485, ISO 9001, TGA standards
Responsibilities
Perform inspections on incoming materials and finished goods, Manage non-conforming materials including documentation and segregation, Support QMS activities and ensure compliance with ISO standards, Handle customer complaints and returns, Maintain accurate quality records and audit documentation, Coordinate MRB activities and ERP inventory movements, Assist with supplier quality issues and CAPA processes, Train staff on SOPs and quality procedures
Seniority
Mid-level (3–5 years experience)